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JP4953519B2 - Masking material for painting - Google Patents

Masking material for painting Download PDF

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Publication number
JP4953519B2
JP4953519B2 JP2001164643A JP2001164643A JP4953519B2 JP 4953519 B2 JP4953519 B2 JP 4953519B2 JP 2001164643 A JP2001164643 A JP 2001164643A JP 2001164643 A JP2001164643 A JP 2001164643A JP 4953519 B2 JP4953519 B2 JP 4953519B2
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Japan
Prior art keywords
masking material
nylon
polyamide
weight
polymer alloy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
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JP2001164643A
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Japanese (ja)
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JP2002187961A (en
Inventor
正則 小川
邦矩 伊藤
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Nagoya Oil Chemical Co Ltd
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Nagoya Oil Chemical Co Ltd
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Priority to JP2001164643A priority Critical patent/JP4953519B2/en
Application filed by Nagoya Oil Chemical Co Ltd filed Critical Nagoya Oil Chemical Co Ltd
Priority to US10/399,078 priority patent/US7247366B2/en
Priority to KR1020037005108A priority patent/KR100791915B1/en
Priority to CA002424080A priority patent/CA2424080C/en
Priority to PCT/JP2001/008771 priority patent/WO2002030580A1/en
Priority to AU2001294189A priority patent/AU2001294189B2/en
Priority to CNB018172318A priority patent/CN1209200C/en
Priority to AU9418901A priority patent/AU9418901A/en
Priority to EP01974696A priority patent/EP1332801A4/en
Priority to TW90124636A priority patent/TW557232B/en
Priority to BR0201228-6A priority patent/BR0201228A/en
Publication of JP2002187961A publication Critical patent/JP2002187961A/en
Application granted granted Critical
Publication of JP4953519B2 publication Critical patent/JP4953519B2/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C08L81/02Polythioethers; Polythioether-ethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05BSPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
    • B05B12/00Arrangements for controlling delivery; Arrangements for controlling the spray area
    • B05B12/16Arrangements for controlling delivery; Arrangements for controlling the spray area for controlling the spray area
    • B05B12/20Masking elements, i.e. elements defining uncoated areas on an object to be coated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • C08L53/025Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes modified
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L71/00Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
    • C08L71/08Polyethers derived from hydroxy compounds or from their metallic derivatives
    • C08L71/10Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
    • C08L71/12Polyphenylene oxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06Polyamides derived from polyamines and polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D153/00Coating compositions based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D153/02Vinyl aromatic monomers and conjugated dienes
    • C09D153/025Vinyl aromatic monomers and conjugated dienes modified
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J153/00Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
    • C09J153/02Vinyl aromatic monomers and conjugated dienes
    • C09J153/025Vinyl aromatic monomers and conjugated dienes modified
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/04Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/14Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/14Layer or component removable to expose adhesive
    • Y10T428/1462Polymer derived from material having at least one acrylic or alkacrylic group or the nitrile or amide derivative thereof [e.g., acrylamide, acrylate ester, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24628Nonplanar uniform thickness material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/28Web or sheet containing structurally defined element or component and having an adhesive outermost layer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31909Next to second addition polymer from unsaturated monomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31931Polyene monomer-containing

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Manufacturing & Machinery (AREA)
  • Details Or Accessories Of Spraying Plant Or Apparatus (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)

Description

【0001】
【産業上の利用分野】
本発明は塗装の際に被塗物の所定位置に該塗装が及ぼされないように、該所定位置を保護するために用いられる塗装用マスキング材に関するものである。
【0002】
【従来の技術】
塗装に際しては被塗物に存在する塗装が施されるべきではない個所(マスキング個所)にマスキング材が取付けられる。該マスキング材は塗装後加熱処理によって塗膜が乾燥硬化して流動性を消失した後で取はずされる。したがってマスキング材はこのような塗装工程における加熱処理に耐えるものでなければならない。
【0003】
このようなマスキング材としては従来、無機充填材を混合した熱可塑性プラスチックを材料とするものが提供されている(特開平2−126966号)。熱可塑性プラスチック材料のうちでも特にポリオレフィンは耐溶剤性に富み、また無機充填材を混合することによって該ポリオレフィンが機械的に補強され、更に熱伝導率が高くなって耐熱性が向上するので、上記マスキング材は塗装工程において繰返し使用することが可能である。
【0004】
しかしながら上記従来のマスキング材にあっては、無機充填材を熱可塑性プラスチックに混合しても耐熱性は高々100℃程度であり、それ以上の温度での加熱処理を要求される塗装工程の場合では、マスキング材が変形してしまい繰返し使用が出来なくなると云う問題点があった。
【0005】
このような問題点を解決するための手段として、エンジニアリングプラスチックを材料とするマスキング材が提供された(特平5−261323)。エンジニアリングプラスチックを材料とするマスキング材は150℃以上の高温加熱処理にも耐え、このような高温加熱処理を含む塗装工程においても繰返し使用が可能である。
【0006】
【発明が解決しようとする課題】
しかしながら、上記エンジニアリングプラスチックは軟化点が高く溶融物の流動性も悪いので成形性に劣ること、硬度が高く脆性を有するからある程度大きな外力が及ぼされると亀裂、割れ等の破壊が生ずるおそれがあること、塗膜との密着性に乏しくマスキング材表面に形成された塗膜が剥離して飛散し、周囲に付着して汚染すると云う問題点があった。
【0007】
【課題を解決するための手段】
本発明は上記従来の課題を解決するための手段として、メチルペンテンコポリマー、ポリスルホン、ポリエーテルスルホン、ポリフェニレンスルフィド、ポリフェニレンエーテル、ポリアミドイミド、ポリエーテルイミド、ポリエーテルエーテルケトンからなる組から選ばれるエンジニアリングプラスチックの一種または二種以上と、ポリアミドおよび/またはポリスチレンと、スチレン系熱可塑性エラストマーとを含有するポリマーアロイであって、該エンジニアリングプラスチックと該ポリアミドおよび/またはポリスチレンとは30:70〜70:30重量比で混合され、該スチレン系熱可塑性エラストマーは該エンジニアリングプラスチックと該ポリアミドおよび/またはポリスチレンとの合計100重量部に対して2〜20重量部が添加されているポリマーアロイのシートを真空および/または圧空成形することによって製造されるマスキング材(11,21,31,41,51)を提供するものである。該ポリマーアロイのシートの厚みは0.1〜1.5mmであることが望ましい。また該エンジニアリングプラスチックはポリフェニレンエーテルであることが望ましく、該ポリアミドはナイロン6であることが望ましい。また更に該スチレン系熱可塑性エラストマーはスチレン−水素添加ポリオレフィン−スチレンブロック共重合体であることが望ましい。
【0008】
本発明に用いられるエンジニアリングプラスチック(以下エンプラと略称する)とはポリスルホン(PSF)、ポリエーテルスルホン(PES)、ポリフェニレンエーテル(PPE)、ポリフェニレンスルフィド(PPS)、ポリエーテルエーテルケトン(PEEK)、ポリアミドイミド(PAI)、ポリエーテルイミド(PEI)、メチルペンテンコポリマー(TPX)が選択される。上記エンプラは二種以上混合されてもよい。上記エンプラのうち望ましいものは成形性の点からみてPPEである。
【0009】
本発明においては、上記エンプラにポリアミドおよび/またはポリスチレンが添加される。上記ポリアミドとしては、例えばポリテトラメチレンアジパミド(ナイロン46)、ポリヘキサメチレンアジパミド(ナイロン66)、ポリピロソドン(ナイロン4)、ポリカプロラクタム(ナイロン6)、ポリヘプトラクタム(ナイロン7)、ポリカプリラクタム(ナイロン8)、ポリノナノラクタム(ナイロン9)、ポリウンデカ1ラクタム(ナイロン11)、ポリドデカ1ラクタム(ナイロン12)、ポリヘキサメチレンアゼラインアミド(ナイロン69)、ポリヘキサメチレンセバカミド(ナイロン610)、ポリヘキサメチレンフタルアミド(ナイロン6iP)、ポリヘキサメチレンテレフタルアミド、ポリヘキサメチレンイソフタルアミド、ポリテトラメチレンイソフタルアミド、ポリメタキシレンアジパミド、ナイロンMSD6、ヘキサメチレンジアミンとn−ドデカン二酸のポリアミド(ナイロン612)、ドデカメチレンジアミンとn−ドデカン二酸のポリアミド(ナイロン1212)、ヘキサメチレンアジパミド/カプロラクタム(ナイロン66/6)、ヘキサメチレンアジパミド/ヘキサメチレンイソフタルアミド(ナイロン66/6iP)、ヘキサメチレンアジパミド/ヘキサメチレンテレフタルアミド(ナイロン66/6T)、トリメチルヘキサメチレンオキサミド/ヘキサメチレンオキサミド、(ナイロントリメチル−62/62)、ヘキサメチレンアジパミド/ヘキサメチレンアゼラインアミド(ナイロン66/69)、ヘキサメチレンアジパミド/ヘキサメチレンアゼラインアミド/カプロラクタム(ナイロン66/69/6)、ポリ(カプロアミド/ヘキサメチレンセバカミド)(ナイロン6/610)、ポリ(カプロアミド/ヘキサメチレンドデカミド)(ナイロン6/612)ナイロンMXD6、ポリ(カプロアミド/ヘキサメチレンイソフタルアミド)(ナイロン6/6I)、芳香族ポリアミド等のポリアミドがある。上記ポリアミドは二種以上混合使用されてもよい。
望ましいポリアミドとしては、ナイロン6、ナイロン66、ナイロン610、ナイロン11、ナイロン12である。上記ポリアミドはポリマーアロイに強靱性を与え、真空および/または圧空成形等による深絞り成形を容易ならしめる。
【0010】
本発明において使用されるポリスチレンとしては、一般用、耐衝撃用のいづれも含まれるが、耐衝撃用ポリスチレンが望ましい。
本発明においては、更にスチレン系熱可塑性エラストマーが使用される。該スチレン系熱可塑性エラストマーとしては、スチレン−ブタジエン−スチレンブロック共重合体(SBS)、スチレン−イソプレン−スチレンブロック共重合体(SIS)、α−メチルスチレン−ブタジエン−αメチルスチレンブロック共重合体(α−MeS−Bd−MeS)、αメチルスチレン−イソプレン−α−メチルスチレンブロック共重合体、スチレン−水素添加ポリオレフィン−スチレンブロック共重合体(SEBS)等があり、望ましいスチレン系熱可塑性エラストマーとしては、耐侯性、耐熱性の点からみてSEBSがある。
【0011】
上記エンプラとゴムおよび/またはエラストマーとの混合物には、炭酸カルシウム、炭酸マグネシウム、硫酸バリウム、硫酸カルシウム、亜硫酸カルシウム、燐酸カルシウム、水酸化カルシウム、水酸化マグネシウム、水酸化アルミニウム、酸化マグネシウム、酸化チタン、酸化鉄、酸化亜鉛、アルミナ、シリカ、ケイ藻土、ドロマイト、石膏、タルク、クレー、アスベスト、マイカ、ガラス繊維、カーボン繊維、ケイ酸カルシウム、炭酸カルシウム、ベンナイト、ホワイトカーボン、カーボンブラック、鉄粉、アルミニウム粉、石粉、高炉スラグ、フライアッシュ、セメント、ジルコニア粉等の無機充填材、木綿、麻、竹繊維、ヤシ繊維、羊毛等の天然繊維、ポリアミド繊維、ポリエステル繊維、アクリル繊維、ビスコース繊維、アセテート繊維、塩化ビニル繊維、塩化ビニリデン繊維等の有機合成繊維、アスベスト繊維、ガラス繊維、炭素繊維、セラミック繊維、金属繊維、ウィスカー等の無機繊維、リンター、リネン、サイザル、木粉、ヤシ粉、クルミ粉、でん粉、小麦粉等の有機充填材等の補強材を添加して形状保持性、寸法安定性、圧縮および引張強度等を向上せしめてもよい。上記充填材は通常上記エンプラに対して0.5〜200重量%程度添加される。
【0012】
上記ポリマーアロイには更に必要に応じ更にポリエチレン、ポリプロピレン、エチレン−プロピレン共重合体、エチレン−酢酸ビニル共重合体等のポリオレフィン、塩化ビニル系樹脂、アクリル系樹脂、メタクリレート系樹脂、塩化ビニリデン系樹脂、プロピオン酸ビニル系樹脂、スチレン−ブタジエン共重合体、ポリエステル系樹脂等の熱可塑性プラスチックの一種または二種以上が混合されてもよい。
【0013】
上記ポリマーアロイには、またマスキング部位識別のために顔料や染料等により着色され色分けされてもよく、更にまたDOP,DBP等の可塑剤、酸化防止剤、帯電防止剤、結晶化促進剤、難燃剤、防炎剤、防虫剤、防腐剤、ワックス類、滑剤、老化防止剤、紫外線吸収剤、化学発泡剤またはカプセル型発泡剤のような発泡剤等を添加してもよい。これらの成分は一種または二種以上相互に混合して添加せられてもよい。
【0014】
上記ポリマーアロイによりマスキング材を製造するには通常フィルム状もしくはシ−ト状にして真空成形あるいは真空圧空成形を行ない所定形状に成形する方法が深絞り形状や複雑形状が正確に成形出来、また大量生産にもっとも適した方法ではあるが、それ以外に、圧空成形、プレス成形、ブロー成形、射出成形等が適用されてもよい。
上記ポリマーアロイのシートには更にポリエチレン、ポリプロピレン、エチレン−プロピレン共重合体、エチレン−酢酸ビニル共重合体等のポリオレフィン、塩化ビニル系樹脂、アクリル系樹脂、メタクリレート系樹脂、塩化ビニリデン系樹脂、スチレン系樹脂、プロピオン酸ビニル系樹脂、スチレン−ブタジエン共重合体、ポリエステル系樹脂等の熱可塑性プラスチックのシートまたは該熱可塑性プラスチックの発泡体のシートが積層されてもよい。
【0015】
上記ポリマーアロイからなるマスキング材の表面の一部または全部には例えばコロナ放電処理やプライマー処理等の処理を行なって塗料や接着剤に対する親和性を更に高めてもよい。上記プライマー処理に用いられるプライマーとしては塩素化ポリプロピレン、エチレン−酢酸ビニル共重合体のような変性ポリオレフィンまたはオレフィン共重合体、スチレン−ブタジエンゴム、アクリロニトリル−ブタジエンゴム、クロロプレンゴム、ポリブタジエンのような合成ゴム、アクリル系合成樹脂、ビニル系合成樹脂あるいはアミノ基、アミド基等を含むアクリル系合成樹脂、ビニル系合成樹脂、アミノ系合成樹脂やエポキシ樹脂等の合成ゴムまたは合成樹脂系のプライマー、あるいはアルミニウムイソプロピレート、アルミニウムトリスアセチルアセトネート等のアルミニウムアルコラートまたはアルミニウムキレート化合物、2−エチルヘキシル鉛、ヘキサデシルリチウム等のアルキル金属、ジブチルスズジアセテート、ジ−n−ブチルスズジオキシド等の有機スズ化合物、メチルビニルジクロロシラン等のシラン化合物、アセチルアセトンリチウム、アセチルアセトンベリリウム等の1,3−ジカルボニルの金属錯塩、テトラブチルチタネート等の有機チタン化合物、ホウ酸トリ−n−ブチル、ホウ酸トリフェニル等のホウ酸化合物、リン酸トリオレイル、リン酸トリデシル等のリン酸エステル、ステアリン酸マグネシウム、ナフテン酸コバルト等のカルボン酸金属塩、n−ドデシルメルカプトカリウム塩等の金属チオアルコラート、2−エチルヘキサンジチオ酸亜鉛等のチオジカルボン酸塩、ジメチルジチオカルバミン酸ニッケル、ジメチルジチオカルバミン酸銅等のジチオカルバミン酸金属塩、ベンゼンスルホン酸ニッケル等のスルホン酸金属塩、ジブチルリン酸バナジウム等の有機リン酸金属塩等の低分子量のプライマーがあり、上記プライマーは一種または二種以上の混合物として用いられる。上記プライマーは上記マスキング材として用いられるエンプラの塗料ビヒクルあるいは接着剤として一般的に用いられるエンプラ以外の合成樹脂との双方に良好な接着性を有する合成樹脂またはゴムあるいは上記各種のプライマーが用いられる。上記プライマーとして特に望ましいものとしては第4級アンモニウム塩を含むアクリル系合成樹脂やアミノ系合成樹脂がある。
【0016】
上記各種のプライマーの一種または二種以上の混合物を用いてプライマー処理を施すには、上記各種のプライマーの一種または二種以上の混合物の溶液またはエマルジョン(ラテックス)を上記マスキング材の表面に塗布し乾燥させる。
上記プライマー処理に先立ち、上記マスキング材本体の表面に親和処理を施してもよい。上記親和処理としては、該表面を若干炭化させて親和性を与える火炎処理や硫酸処理、表面を粗にしかつ若干炭化させるコロナ放電処理等がある。
【0017】
【作用】
エンプラは耐熱性に富み、これを材料とするマスキング材は機械的強度が高く、また150℃以上の温度であっても軟化変形しない。上記エンプラにポリアミドおよび/またはポリスチレンと、スチレン系熱可塑性エラストマーとを混合してポリマーアロイとすると、耐熱性は余り低下することなくマスキング材の成形性が向上し、かつ靱性と伸びが向上してシートの厚みが薄くても(通常0.2〜0.8mm)、シートが破れることなく、真空および/または圧空成形による深絞り成形が容易になる。更にこのような薄いシートで成形したマスキング材でも破壊強度が大巾に向上する。また本発明のポリマーアロイは塗膜との親和性も向上する。
【0018】
【実施例】
〔第1実施例〕
図1〜図4に本発明の第1実施例が示される。本実施例のマスキング材(11)は例えば自動車のセンターピラー(12)のような柱状体のマスキングに使用される。そして該マスキング材(11)は内側にセンターピラー(12)の本体(12A) の嵌合部(11B) を形成した断面コの字型の本体(11A) と、該本体(11A) の両側壁(11C,11C)の下縁に沿って形成された該センターピラー(12)のフランジ(12B,12B) を嵌合するフランジ嵌合部(11D,11D) と、該フランジ嵌合部(11D,11D) から延設された裏当て部(11E,11E) と、上部に延設された上当て部(11F) とからなり、本体(11A)のには長手方向の補強縦リブ(11G) と短手方向の補強横リブ(11H) とが形成されている。該マスキング材(11)はPPE−ナイロン66(40:60重量比)混合物100重量部に10重量部のSEBSを混合し、更に炭酸カルシウム5重量%を混合したポリマーアロイのシート(厚み0.4mm)を真空成形することによって製造される。
上記マスキング材(11)は図2に示すようにセンターピラー(12)の本体(12A) を該マスキング材(11)の嵌合部(11B) に嵌合し、更に該センターピラー(12)側縁のフランジ(12B) を該マスキング材(11)のフランジ嵌合部(11D,11D) に嵌合して仮止めを行なう。
上記仮止めの後、図3に示すように該マスキング材(11)の裏当て部(11E,11E)を折返してセンターピラー(12)の裏当て(12C) に当て、該裏当て部(11E,11E) を粘着テープ(14)やタッカー等で固定する。
このようにして上記マスキング材(11)を図4に示すようにセンターピラー(12)に取付けた後、熱硬化性メラミン−アルキド樹脂塗料等によってマスキング材(11)と共に塗装する。
【0019】
〔第2実施例〕
図5には本発明の第2実施例が示される。本実施例のマスキング材(21)は内側にセンターピラー(22)の本体(22A) の嵌合部(21B) を形成した断面コの字型の本体(21A) と、該本体(21A) の両側壁(21C,21C) の下縁に沿って形成された該センターピラー(22)のフランジ(22B,22B) を嵌合するフランジ嵌合部(21D,21D) と、該フランジ嵌合部(21D,21D) から延設された裏当て部(21E,21E) と、上部に延設された上当て部(21F) とからなり、本体(21A) の周囲には長手方向の補強リブ(21G) と短手方向のリブ(21H) とが形成されているが、第1実施例の場合と異なり本実施例では、長手方向の補強リブ(21G) が断続されている。該マスキング材(21)はPPS−ハイインパクトポリスチレン(50:40重量比)の混合物100重量部に対して15重量部のSBSを添加混合し、更にカーボンブラック3重量%を混合したポリマーアロイのシート(厚み0.3mm)を真空圧空成形することによって製造される。
上記マスキング材(21)は第1実施例のマスキング材(11)と同様にしてピラー(22)の本体(22A) を該マスキング材(21)の嵌合部(21B) に嵌合し、更に該センターピラー(22)側縁のフランジ(22B) を該マスキング材(21)のフランジ嵌合部(21D,21D) に嵌合して仮止めを行ない、該マスキング材(21)の裏当て部(21E,21E) を折返してピラー(22)の裏当てに当て、該裏当て部(21E,21E) を粘着テープやタッカー等で止着する。
このようにして塗料等によってマスキング材(21)と共に塗装する。
第1実施例のマスキング材(11)は長手方向の補強リブ(11G) が連続しているから、該補強リブ(11G) に沿って折り曲がり易かったが、本実施例のマスキング材(21)は長手方向の補強リブ(21G) が断続しているから、リブ(21G) に沿っての折り曲げ剛性が向上する。
【0020】
〔第3実施例〕
図6〜図8に本発明の第3実施例を示す。図6において(33)は自動車の車体であり、塗装に際してはフロントバンパー(34)の下側スカート部(35)の空気取入れ口(36)に本実施例のマスキング材(31)が取付けられる。該スカート部(35)の空気取入れ口(36)の内側には縦横の補強桟(36A,36B) と左右一対の支柱(36C) とが設けられており、該マスキング材(31)には該補強桟(36A,36B) および支柱(36C) を嵌合するための縦横の嵌合溝(32A,32B) および嵌合溝(32C) が形成されており、前面周縁にはフランジ(32D) が形成されており、更に周面には粘着層(32E) が形成されている。
該マスキング材(31)はPPE−ナイロン6(50:50重量比)100重量部に対して8重量部のSISを添加混合した混合物のシート(厚み0.2mm)を真空成形することによって製造される。該マスキング材(31)は該空気取入れ口(36)の内側に嵌着され、該空気取入れ口(36)の補強桟(36A,36B) はマスキング材(31)の嵌合溝(32A,32B) に嵌合され、支柱(36C) は嵌合溝(32C) に嵌合される。そして該マスキング材(31)は粘着層(32E) によって該空気取入れ口(36)の内側に固定される。なお粘着層(32E) は必ずしも形成されなくてもよい。
このようにしてマスキング個所であるスカート部(35)の空気取入れ口(36)にマスキング材(31)を取付けた上で車体(33)を塗装し、該塗装後熱処理によって塗膜を乾燥硬化させる。
【0021】
〔第4実施例〕
図9〜図12に本発明の第4実施例を示す。本実施例のマスキング材(41)は自動車のドア(44)の窓枠(44A) のマスキングに使用され、該マスキング材(41)は断面L字形の3個の部材(41A,41B,41C) からなり、各部材(41A,41B,41C) には長手方向の補強用縦リブ(41D) と短手方向の補強用横リブ(41E) が形成されている。該マスキング材(41)はPPS−ナイロン66(70:30重量比)の混合物100重量部に対してSEBSを20重量部添加混合したポリマーアロイのシート(厚み0.5mm)を真空圧空成形することによって製造される。
該マスキング材(41)をドア(44)の窓枠(44A) に取付けるには、図10に示すように該マスキング材(41)の各部材(41A,41B,41C) を該窓枠(44A) に当接すると共に各部材(41A,41B,41C) の接続部相互を重ね合わせて例えば粘着テープ(42)等で該接続部分を上から固定する。
この場合、図11に示すように各部材(41A,41B,41C) 相互の接続部分において、一方の接続端の横リブ(41E) を他方の接続端の横リブ(41E) の下側に嵌合し、また図12に示すように各部材(41A,41B,41C) の上縁鉤部(41F) を該窓枠(44A)の上縁に引掛ける。
塗装後は該マスキング材(41)をドア(44)の窓枠(44A) から剥離する。該ドア(44)の窓枠(44A) はマスキング材(41)によって保護されていたので塗膜は形成されない。
【0022】
〔第5実施例〕
本発明を図13〜図17に本発明の第5実施例を示す。(52)は自動車のインストルーメントパネルであって、前面にはグローブボックス取付け穴(55)、オーディオ取付け穴(56,57) 、計器類取付部(58)、小物入れ取付部(59)等が設けられており、該インストルーメントパネル(52)は上部(52A) と下部(52B) とに分割されている。
【0023】
該インストルーメントパネル(52)は、図14に示すように基材(54)と、該基材(54)表面に貼着される表装材(53)とからなり、該表装材(53)は不織布、合成皮革等からなる表皮材(53A) と、該表皮材(53A) に裏打ちされている不織布、プラスチック発泡体シート等からなるワディング材(53B) とからなり、該表皮材(53A)は所定の色(基色)に着色されており、該ワディング材(53B) の厚みを弾性的に変化させることが可能である。
【0024】
上部(52A) と下部(52B) との境界に沿って基材(54)には凹溝(54A) が設けられており、表装材(53)はこの部分で該凹溝(54A) 内にきめ込むことによってパーティングラインPLが形成されている。該表装材(53)はきめ込み部分でワディング材(53B) が厚みを圧縮され、その弾性復元力によって凹溝(54A) 内に固定されている。
【0025】
上記インストルーメントパネル(52)は上下共通の表装材(53)によって化粧されているから上下同色(基色)である。これをこのまゝ自動車車体に取付けてもよいが、上下異色にするには図13に示すようなマスキング材(51)を使用する。該マスキング材(51)はインストルーメントパネル(52)上部(52A) に適嵌する形状を有し、端縁部には係合フランジ(51A) が形成されている。
【0026】
該マスキング材(51)は図15に示すように該インストルーメントパネル上部(52A) に被着され、図16に示すように係合フランジ(51A) をパーティングラインPLの隙間Sに挿着することによって固定される。該マスキング材(51)の係合フランジ(51A) をパーティングラインPLの隙間Sに挿着すると、該表装材(53)のワディング材(53B) が厚みを圧縮され、その弾性復元力によって該係合フランジ(51A) が表装材(53)によって挾圧され固定される。
【0027】
マスキング材(51)をインストルーメントパネル上部(52A) に取付けた上で、インストルーメントパネル下部(52B) をスプレー塗装等で上部(52A) とは異色に塗装する。塗装後はマスキング材(51)を取りはずす。このようにして図17に示すような上下異色のインストルーメントパネル(52)が簡単に得られる。
【0028】
本実施例のマスキング材(51)はPPE−ナイロン6(40:60重量比)の混合物100重量部に対して10重量部のSEBSと2重量部の酸化チタンおよび0.5重量部のカーボンブラックとを添加混合したポリマーアロイのシート(厚み0.4mm)を圧空成形することによって製造される。
【0029】
【発明の効果】
耐熱性に優れ、外力によって亀裂、割れ等の破壊が生ずるおそれがなく、成形性、特に深絞り形状や複雑形状が正確に得られ、大量生産にも適した真空成形や真空圧空成形あるいは圧空成形における成形性が良好で被マスキング個所のどのような形状にも対応して成形が出来、しかもこのような真空成形、真空圧空成形あるいは圧空成形においては、薄いシートを原料としても可能であり、したがって材料コストも安くなり、更にマスキング材に形成された塗膜の密着性が良好で、該塗膜が剥離して周囲に飛散することのない塗装用マスキング材が得られる。したがって本発明の塗装用マスキング材は繰返し使用が可能となる。
【図面の簡単な説明】
図1〜図4は本発明の第1実施例を示すものである。
【図1】 斜視図
【図2】 仮止め状態の図4におけるA−A断面図
【図3】 固定状態の図4におけるA−A断面図
【図4】 ピラー取付状態斜視図
【図5】 第2実施例の斜視図図6〜図8は第3実施例を示すものである。
【図6】 斜視図
【図7】 マスキング材取付状態の横断面図
【図8】 マスキング材取付状態の縦断面図
図9〜12は本発明の第4実施例を示すものである。
【図9】 斜視図
【図10】 マスキング材取付状態斜視図
【図11】 図10におけるA−A断面図
【図12】 図10におけるB−B断面図
図13〜図17は本発明の第5実施例を示すものである。
【図13】 塗装前のインストルーメントパネルとマスキング材の斜視図
【図14】 図13におけるA−A断面図
【図15】 マスキング材被着塗装状態の斜視図
【図16】 図15におけるB−B断面図
【図17】 異色インストルーメントパネルの斜視図
【符号の説明】
11,21,31,41,51 マスキング材
[0001]
[Industrial application fields]
The present invention relates to a coating masking material used for protecting a predetermined position so that the coating is not applied to a predetermined position of an object to be coated.
[0002]
[Prior art]
At the time of painting, a masking material is attached to a portion (masking portion) that should not be painted on the object to be coated. The masking material is removed after the coating film is dried and cured by heat treatment after coating and loses fluidity. Therefore, the masking material must be able to withstand the heat treatment in such a painting process.
[0003]
As such a masking material, there is conventionally provided a material made of a thermoplastic plastic mixed with an inorganic filler (Japanese Patent Laid-Open No. 2-126966). Among thermoplastic materials, especially polyolefin is rich in solvent resistance, and by mixing an inorganic filler, the polyolefin is mechanically reinforced, and the thermal conductivity is increased to improve heat resistance. The masking material can be used repeatedly in the painting process.
[0004]
However, in the conventional masking material, heat resistance is at most about 100 ° C. even when an inorganic filler is mixed with thermoplastic, and in the case of a coating process that requires heat treatment at a temperature higher than that. There is a problem that the masking material is deformed and cannot be used repeatedly.
[0005]
To solve this problem, the masking material for engineering plastics and materials have been provided (Japanese open flat 5-261323). Masking materials made of engineering plastics can withstand high-temperature heat treatment at 150 ° C. or higher, and can be used repeatedly in coating processes including such high-temperature heat treatment.
[0006]
[Problems to be solved by the invention]
However, the engineering plastic has a high softening point and poor flowability of the melt, so it is inferior in moldability, and because it has high hardness and brittleness, it may cause fracture such as cracks and cracks when a large external force is applied. The coating film formed on the surface of the masking material with poor adhesion to the coating film peels off and scatters and adheres to the surrounding area to cause contamination.
[0007]
[Means for Solving the Problems]
The present invention provides an engineering plastic selected from the group consisting of methylpentene copolymer, polysulfone, polyethersulfone, polyphenylene sulfide, polyphenylene ether, polyamideimide, polyetherimide, and polyetheretherketone as means for solving the above conventional problems. A polymer alloy containing one or more of the following, polyamide and / or polystyrene, and a styrenic thermoplastic elastomer, wherein the engineering plastic and the polyamide and / or polystyrene are 30:70 to 70:30 weight The styrenic thermoplastic elastomer is mixed in a ratio of 2 to 20 parts by weight with respect to a total of 100 parts by weight of the engineering plastic and the polyamide and / or polystyrene. A sheet of a polymer alloy which is added is to provide a masking material which is produced by vacuum and / or pressure forming (11,21,31,41,51). Sheet having a thickness of the polymer alloy is preferably a 0.1 to 1.5 mm. The engineering plastic is preferably polyphenylene ether, and the polyamide is preferably nylon 6. Furthermore, it is desirable that the styrenic thermoplastic elastomer is a styrene-hydrogenated polyolefin-styrene block copolymer.
[0008]
The engineering plastic (hereinafter abbreviated as engineering plastic) used in the present invention is polysulfone (PSF), polyethersulfone (PES), polyphenylene ether (PPE), polyphenylene sulfide (PPS), polyetheretherketone (PEEK), polyamideimide. (PAI), polyetherimide (PEI), methylpentene copolymer (TPX) are selected. Two or more of the above engineering plastics may be mixed. Of the above engineering plastics, PPE is preferable from the viewpoint of moldability.
[0009]
In the present invention, polyamide and / or polystyrene is added to the engineering plastic. Examples of the polyamide include polytetramethylene adipamide (nylon 46), polyhexamethylene adipamide (nylon 66), polypyrosodon (nylon 4), polycaprolactam (nylon 6), polyheptlactam (nylon 7), Polycaprylactam (nylon 8), Polynonanolactam (nylon 9), Polyundeca 1 lactam (nylon 11), Polydodeca 1 lactam (nylon 12), Polyhexamethylene azelainamide (nylon 69), Polyhexamethylene sebacamide (nylon) 610), polyhexamethylene phthalamide (nylon 6iP), polyhexamethylene terephthalamide, polyhexamethylene isophthalamide, polytetramethylene isophthalamide, polymetaxylene adipamide, nylon MSD , Polyamide of hexamethylene diamine and n-dodecanedioic acid (nylon 612), polyamide of dodecane diamine and n-dodecanedioic acid (nylon 1212), hexamethylene adipamide / caprolactam (nylon 66/6), hexamethylene azimuth Pamide / hexamethylene isophthalamide (nylon 66 / 6iP), hexamethylene adipamide / hexamethylene terephthalamide (nylon 66 / 6T), trimethylhexamethylene oxamide / hexamethylene oxamide, (nylon trimethyl-62 / 62) , Hexamethylene adipamide / hexamethylene azelainamide (nylon 66/69), hexamethylene adipamide / hexamethylene azelainamide / caprolactam (nylon 66/69/6), poly (caproa) Dom / hexamethylene sebacamide) (nylon 6/610), poly (caproamide / hexamethylene dodecamide) (nylon 6/612) nylon MXD6, poly (caproamide / hexamethylene isophthalamide) (nylon 6 / 6I), aroma There are polyamides such as group polyamides. Two or more of the above polyamides may be used in combination.
Desirable polyamides are nylon 6, nylon 66, nylon 610, nylon 11, and nylon 12. The polyamide imparts toughness to the polymer alloy and facilitates deep drawing by vacuum and / or pressure forming.
[0010]
The polystyrene used in the present invention includes both general-purpose and impact-resistant polystyrene, but impact-resistant polystyrene is desirable.
In the present invention, a styrenic thermoplastic elastomer is further used. Examples of the styrenic thermoplastic elastomer include styrene-butadiene-styrene block copolymer (SBS), styrene-isoprene-styrene block copolymer (SIS), α-methylstyrene-butadiene-α-methylstyrene block copolymer ( α-MeS-Bd-MeS), α-methylstyrene-isoprene-α-methylstyrene block copolymer, styrene-hydrogenated polyolefin-styrene block copolymer (SEBS), etc. There is SEBS in terms of weather resistance and heat resistance.
[0011]
The above engineering plastic and rubber and / or elastomer mixture includes calcium carbonate, magnesium carbonate, barium sulfate, calcium sulfate, calcium sulfite, calcium phosphate, calcium hydroxide, magnesium hydroxide, aluminum hydroxide, magnesium oxide, titanium oxide, Iron oxide, zinc oxide, alumina, silica, diatomaceous earth, dolomite, gypsum, talc, clay, asbestos, mica, glass fiber, carbon fiber, calcium silicate, calcium carbonate, bennite, white carbon, carbon black, iron powder, Inorganic fillers such as aluminum powder, stone powder, blast furnace slag, fly ash, cement, zirconia powder, natural fibers such as cotton, hemp, bamboo fiber, palm fiber, wool, polyamide fiber, polyester fiber, acrylic fiber, viscose fiber, Acetate Organic synthetic fibers such as fiber, vinyl chloride fiber, vinylidene chloride fiber, asbestos fiber, glass fiber, carbon fiber, ceramic fiber, metal fiber, whisker and other inorganic fibers, linter, linen, sisal, wood powder, palm powder, walnut powder A reinforcing material such as an organic filler such as starch or wheat flour may be added to improve shape retention, dimensional stability, compression and tensile strength, and the like. The filler is usually added in an amount of about 0.5 to 200% by weight with respect to the engineering plastic.
[0012]
If necessary, the above polymer alloy further includes polyolefin such as polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-vinyl acetate copolymer, vinyl chloride resin, acrylic resin, methacrylate resin, vinylidene chloride resin, One kind or two or more kinds of thermoplastic plastics such as vinyl propionate resin, styrene-butadiene copolymer, and polyester resin may be mixed.
[0013]
The above polymer alloy may be colored with a pigment or a dye to identify a masking site, and may be color-coded. Further, a plasticizer such as DOP or DBP, an antioxidant, an antistatic agent, a crystallization accelerator, a difficult A foaming agent such as a flame retardant, a flameproofing agent, an insecticide, an antiseptic, a wax, a lubricant, an antiaging agent, an ultraviolet absorber, a chemical foaming agent or a capsule type foaming agent may be added. These components may be added singly or in combination of two or more.
[0014]
In order to manufacture a masking material by the above polymer alloy, a method of forming a predetermined shape by performing vacuum forming or vacuum / pressure forming in a film or sheet can be accurately formed, and a large amount can be formed. Although it is the most suitable method for production, other than that, pressure forming, press forming, blow molding, injection molding, etc. may be applied.
Polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-vinyl acetate copolymer and other polyolefins, vinyl chloride resin, acrylic resin, methacrylate resin, vinylidene chloride resin, styrene A sheet of a thermoplastic plastic such as a resin, a vinyl propionate resin, a styrene-butadiene copolymer, a polyester resin, or a foamed sheet of the thermoplastic plastic may be laminated.
[0015]
A part or all of the surface of the masking material made of the polymer alloy may be subjected to a treatment such as a corona discharge treatment or a primer treatment to further enhance the affinity for the paint or adhesive. Primers used in the above primer treatment include chlorinated polypropylene, modified polyolefin or olefin copolymer such as ethylene-vinyl acetate copolymer, styrene-butadiene rubber, acrylonitrile-butadiene rubber, chloroprene rubber, and synthetic rubber such as polybutadiene. Acrylic synthetic resins, vinyl synthetic resins or acrylic synthetic resins containing amino groups, amide groups, etc., vinyl synthetic resins, synthetic rubbers such as amino synthetic resins and epoxy resins, or synthetic resin primers, or aluminum isopropyl Rate, aluminum alcoholate or aluminum chelate compound such as aluminum trisacetylacetonate, alkyl metal such as 2-ethylhexyl lead, hexadecyl lithium, dibutyltin diacetate, di Organotin compounds such as n-butyltin dioxide, silane compounds such as methylvinyldichlorosilane, metal complex salts of 1,3-dicarbonyl such as acetylacetone lithium and acetylacetone beryllium, organotitanium compounds such as tetrabutyltitanate, triborate borate Boric acid compounds such as n-butyl and triphenyl borate, phosphate esters such as trioleyl phosphate and tridecyl phosphate, metal carboxylates such as magnesium stearate and cobalt naphthenate, and n-dodecyl mercapto potassium salt Metal thioalcolate, thiodicarboxylates such as zinc 2-ethylhexanedithioate, dithiocarbamate metal salts such as nickel dimethyldithiocarbamate, copper dimethyldithiocarbamate, metal sulfonates such as nickel benzenesulfonate, dibutyl There are primers low molecular weight such as organic phosphoric acid metal salts such as phosphate vanadium, the primer is used as one or a mixture of two or more. As the primer, a synthetic resin or rubber having good adhesion to both a paint vehicle of engineering plastics used as the masking material and a synthetic resin other than engineering plastics generally used as an adhesive, or the above-mentioned various primers are used. Particularly desirable as the primer is an acrylic synthetic resin or amino synthetic resin containing a quaternary ammonium salt.
[0016]
In order to perform primer treatment using one or a mixture of two or more of the above various primers, a solution or emulsion (latex) of one or two or more of the above various primers is applied to the surface of the masking material. dry.
Prior to the primer treatment, an affinity treatment may be applied to the surface of the masking material body. Examples of the affinity treatment include flame treatment and sulfuric acid treatment for slightly carbonizing the surface to give affinity, corona discharge treatment for roughening and slightly carbonizing the surface, and the like.
[0017]
[Action]
Engineering plastics are rich in heat resistance, and masking materials made of these materials have high mechanical strength and do not soften and deform even at temperatures of 150 ° C. or higher. When polyamide and / or polystyrene and styrene thermoplastic elastomer are mixed with the above engineering plastics to form a polymer alloy, the moldability of the masking material is improved and the toughness and elongation are improved without much lowering the heat resistance. Even if the sheet is thin (usually 0.2 to 0.8 mm), deep drawing by vacuum and / or pressure forming is facilitated without breaking the sheet. Furthermore, even with a masking material formed from such a thin sheet, the breaking strength is greatly improved. The polymer alloy of the present invention also improves the affinity with the coating film.
[0018]
【Example】
[First embodiment]
1 to 4 show a first embodiment of the present invention. The masking material (11) of this embodiment is used for masking a columnar body such as an automobile center pillar (12). The masking material (11) includes a U-shaped main body (11A) having a fitting portion (11B) of the main body (12A) of the center pillar (12) on the inside, and both side walls of the main body (11A). (11C, 11C) flange fitting part (11D, 11D) that fits the flange (12B, 12B) of the center pillar (12) formed along the lower edge, and the flange fitting part (11D, 11D) is composed of a backing part (11E, 11E) extended from the upper part and an upper backing part (11F) extended to the upper part, and the main body (11A) has longitudinal reinforcing longitudinal ribs (11G) and Reinforcing transverse ribs (11H) in the short direction are formed. The masking material (11) is a polymer alloy sheet (thickness 0.4 mm) obtained by mixing 10 parts by weight of SEBS with 100 parts by weight of a PPE-nylon 66 (40:60 weight ratio) mixture and further mixing 5% by weight of calcium carbonate. ) By vacuum forming.
As shown in FIG. 2, the masking material (11) fits the body (12A) of the center pillar (12) into the fitting portion (11B) of the masking material (11), and further the center pillar (12) side. The edge flange (12B) is temporarily fitted to the flange fitting portions (11D, 11D) of the masking material (11).
After the temporary fixing, as shown in FIG. 3, the backing portions (11E, 11E) of the masking material (11) are folded and applied to the backing (12C) of the center pillar (12), and the backing portions (11E , 11E) is fixed with adhesive tape (14) or tucker.
In this way, after the masking material (11) is attached to the center pillar (12) as shown in FIG. 4, it is applied together with the masking material (11) with a thermosetting melamine-alkyd resin paint or the like.
[0019]
[Second Embodiment]
FIG. 5 shows a second embodiment of the present invention. The masking material (21) of this example is a U-shaped main body (21A) having a fitting portion (21B) of the main body (22A) of the center pillar (22) on the inside, and the main body (21A) Flange fitting portions (21D, 21D) for fitting the flanges (22B, 22B) of the center pillar (22) formed along the lower edges of the side walls (21C, 21C), and the flange fitting portions ( 21D, 21D) consists of a backing part (21E, 21E) and an upper part (21F) extended to the top, and around the body (21A), there are longitudinal reinforcing ribs (21G ) And a short rib (21H), but unlike the first embodiment, the longitudinal reinforcing rib (21G) is intermittent in this embodiment. The masking material (21) is a sheet of polymer alloy in which 15 parts by weight of SBS is added to and mixed with 100 parts by weight of a PPS-high impact polystyrene (50:40 weight ratio) mixture, and 3% by weight of carbon black is further mixed. Manufactured by vacuum-pressure forming (thickness 0.3 mm).
In the same manner as the masking material (11) of the first embodiment, the masking material (21) fits the main body (22A) of the pillar (22) into the fitting portion (21B) of the masking material (21). The flange (22B) on the side edge of the center pillar (22) is fitted to the flange fitting portion (21D, 21D) of the masking material (21) to be temporarily fixed, and the backing portion of the masking material (21) (21E, 21E) is folded and applied to the backing of the pillar (22), and the backing (21E, 21E) is fastened with an adhesive tape, a tucker or the like.
In this way, it is applied together with the masking material (21) by a paint or the like.
The masking material (11) of the first embodiment is easily bent along the reinforcing rib (11G) because the longitudinal reinforcing ribs (11G) are continuous, but the masking material (21) of this embodiment is easy to bend. Since the reinforcing rib (21G) in the longitudinal direction is intermittent, the bending rigidity along the rib (21G) is improved.
[0020]
[Third embodiment]
6 to 8 show a third embodiment of the present invention. In FIG. 6, (33) is a car body, and the masking material (31) of this embodiment is attached to the air intake (36) of the lower skirt part (35) of the front bumper (34) when painting. Vertical and horizontal reinforcing bars (36A, 36B) and a pair of left and right columns (36C) are provided inside the air intake port (36) of the skirt portion (35), and the masking material (31) has the Vertical and horizontal fitting grooves (32A, 32B) and fitting grooves (32C) for fitting the reinforcing bars (36A, 36B) and struts (36C) are formed, and a flange (32D) is formed on the front periphery. In addition, an adhesive layer (32E) is formed on the peripheral surface.
The masking material (31) is manufactured by vacuum forming a sheet (thickness 0.2 mm) of a mixture in which 8 parts by weight of SIS is added to 100 parts by weight of PPE-nylon 6 (50:50 weight ratio). The The masking material (31) is fitted inside the air intake port (36), and the reinforcing bars (36A, 36B) of the air intake port (36) are fitted into the fitting grooves (32A, 32B) of the masking material (31). ) And the column (36C) is fitted into the fitting groove (32C). The masking material (31) is fixed inside the air intake port (36) by the adhesive layer (32E). Note that the adhesive layer (32E) is not necessarily formed.
In this way, after attaching the masking material (31) to the air intake port (36) of the skirt portion (35) which is the masking part, the vehicle body (33) is painted, and the coating film is dried and cured by heat treatment after the coating. .
[0021]
[Fourth embodiment]
9 to 12 show a fourth embodiment of the present invention. The masking material (41) of the present embodiment is used for masking the window frame (44A) of the automobile door (44), and the masking material (41) has three members (41A, 41B, 41C) having an L-shaped cross section. Each member (41A, 41B, 41C) is formed with longitudinal reinforcing ribs (41D) and transverse reinforcing ribs (41E) in the short direction. The masking material (41) is formed by vacuum / pressure forming a polymer alloy sheet (thickness 0.5 mm) in which 20 parts by weight of SEBS is added to 100 parts by weight of a mixture of PPS-nylon 66 (70:30 weight ratio). Manufactured by.
In order to attach the masking material (41) to the window frame (44A) of the door (44), as shown in FIG. 10, each member (41A, 41B, 41C) of the masking material (41) is attached to the window frame (44A). ) And the connecting portions of the members (41A, 41B, 41C) are overlapped with each other, and the connecting portions are fixed from above with, for example, an adhesive tape (42).
In this case, as shown in FIG. 11, in the connection portion between the members (41A, 41B, 41C), the horizontal rib (41E) at one connection end is fitted below the horizontal rib (41E) at the other connection end. Further, as shown in FIG. 12, the upper edge flange portion (41F) of each member (41A, 41B, 41C) is hooked on the upper edge of the window frame (44A).
After painting, the masking material (41) is peeled from the window frame (44A) of the door (44). Since the window frame (44A) of the door (44) is protected by the masking material (41), no coating film is formed.
[0022]
[Fifth embodiment]
The fifth embodiment of the present invention is shown in FIGS. (52) is the instrument panel of the car, and the front has glove box mounting holes (55), audio mounting holes (56, 57), instrument mounting parts (58), accessory case mounting parts (59), etc. The instrument panel (52) is divided into an upper part (52A) and a lower part (52B).
[0023]
As shown in FIG. 14, the instrument panel (52) includes a base material (54) and a surface material (53) adhered to the surface of the base material (54). A skin material (53A) made of a nonwoven fabric, synthetic leather, etc., and a wadding material (53B) made of a nonwoven fabric, plastic foam sheet, etc. backed by the skin material (53A), the skin material (53A) It is colored in a predetermined color (base color), and the thickness of the wadding material (53B) can be changed elastically.
[0024]
A concave groove (54A) is provided in the base material (54) along the boundary between the upper part (52A) and the lower part (52B), and the cover material (53) is placed in the concave groove (54A) at this part. The parting line PL is formed by tightening. In the cover material (53), the thickness of the wadding material (53B) is compressed at the crimped portion, and is fixed in the concave groove (54A) by its elastic restoring force.
[0025]
The instrument panel (52) has the same upper and lower colors (base color) because the instrument panel (52) is decorated with a common upper and lower cover material (53). This may be attached to the car body as it is, but a masking material (51) as shown in FIG. The masking material (51) has a shape that fits in the upper part (52A) of the instrument panel (52), and an engaging flange (51A) is formed at the end edge.
[0026]
The masking material (51) is attached to the upper part (52A) of the instrument panel as shown in FIG. 15, and the engaging flange (51A) is inserted into the gap S of the parting line PL as shown in FIG. Fixed by. When the engaging flange (51A) of the masking material (51) is inserted into the gap S of the parting line PL, the thickness of the wadding material (53B) of the cover material (53) is compressed, and the elastic restoring force causes the The engaging flange (51A) is pressed and fixed by the cover material (53).
[0027]
After attaching the masking material (51) to the upper part of the instrument panel (52A), the lower part of the instrument panel (52B) is painted differently from the upper part (52A) by spray painting or the like. Remove the masking material (51) after painting. In this way, an instrument panel (52) having different colors as shown in FIG. 17 can be easily obtained.
[0028]
The masking material (51) of this example is 10 parts by weight of SEBS, 2 parts by weight of titanium oxide and 0.5 parts by weight of carbon black with respect to 100 parts by weight of a mixture of PPE-nylon 6 (40:60 weight ratio). the sheet (thickness 0.4 mm) of a polymer alloy obtained by mixing added bets are made by pressure forming forms to Rukoto.
[0029]
【Effect of the invention】
Excellent heat resistance, there is no risk of breakage such as cracks and cracks due to external force, moldability, especially deep drawing shape and complicated shape can be obtained accurately, vacuum forming, vacuum pressure forming or pressure forming suitable for mass production In this vacuum forming, vacuum pressure forming or pressure forming, it is possible to use a thin sheet as a raw material. material cost becomes cheaper, further has good adhesion of the coating film formed on the masking material, it no paint masking material coating film is scattered around and peeling can be obtained. Therefore, the coating masking material of the present invention can be used repeatedly.
[Brief description of the drawings]
1 to 4 show a first embodiment of the present invention.
FIG. 1 is a perspective view .
FIG. 2 is a cross-sectional view taken along line AA in FIG . 4 in a temporarily fixed state .
3 is a cross-sectional view taken along line AA in FIG . 4 in a fixed state .
FIG. 4 is a perspective view of a pillar mounting state .
FIG. 5 is a perspective view of the second embodiment. FIGS. 6 to 8 show the third embodiment.
FIG. 6 is a perspective view .
FIG. 7 is a cross-sectional view of the masking material attached state .
FIG. 8 is a longitudinal sectional view of a masking material attached state .
9 to 12 show a fourth embodiment of the present invention.
FIG. 9 is a perspective view .
FIG. 10 is a perspective view of a masking material attached state .
11 is a cross-sectional view taken along line AA in FIG .
12 is a sectional view taken along line BB in FIG .
13 to 17 show a fifth embodiment of the present invention.
FIG. 13 is a perspective view of an instrument panel and a masking material before painting .
14 is a cross-sectional view taken along line AA in FIG .
FIG. 15 is a perspective view of a masking material coating state .
16 is a cross-sectional view taken along the line BB in FIG .
FIG. 17 is a perspective view of a different color instrument panel .
[Explanation of symbols]
11,21,31,41,51 Masking material .

Claims (5)

メチルペンテンコポリマー、ポリスルホン、ポリエーテルスルホン、ポリフェニレンスルフィド、ポリフェニレンエーテル、ポリアミドイミド、ポリエーテルイミド、ポリエーテルエーテルケトンからなる組から選ばれるエンジニアリングプラスチックの一種または二種以上と、ポリアミドおよび/またはポリスチレンと、スチレン系熱可塑性エラストマーとを含有するポリマーアロイであって、該エンジニアリングプラスチックと該ポリアミドおよび/またはポリスチレンとは30:70〜70:30重量比で混合され、該スチレン系熱可塑性エラストマーは該エンジニアリングプラスチックと該ポリアミドおよび/またはポリスチレンとの合計100重量部に対して2〜20重量部が添加されているポリマーアロイのシートを真空および/または圧空成形することによって製造されることを特徴とする塗装用マスキング材 One or more engineering plastics selected from the group consisting of methylpentene copolymer, polysulfone, polyethersulfone, polyphenylene sulfide, polyphenylene ether, polyamideimide, polyetherimide, polyetheretherketone, polyamide and / or polystyrene, A polymer alloy containing a styrenic thermoplastic elastomer, wherein the engineering plastic and the polyamide and / or polystyrene are mixed in a weight ratio of 30:70 to 70:30, and the styrenic thermoplastic elastomer is the engineering plastic. vacuum and with the polyamide and / or polystyrene as the sum of the polymer alloy 2-20 parts by weight are added per 100 parts by weight of the sheet Or pressure forming paint masking material, characterized in that it is manufactured by. 該ポリマーアロイのシートの厚みは0.1〜1.5mmである請求項に記載の塗装用マスキング材 The coating masking material according to claim 1 , wherein the polymer alloy sheet has a thickness of 0.1 to 1.5 mm . 該エンジニアリングプラスチックはポリフェニレンエーテルである請求項1または請求項2に記載の塗装用マスキング材 The coating masking material according to claim 1 or 2 , wherein the engineering plastic is polyphenylene ether . 該ポリアミドはナイロン6である請求項1〜3のいずれか1項に記載の塗装用マスキング材 The masking material for coating according to any one of claims 1 to 3 , wherein the polyamide is nylon 6 . 該スチレン系熱可塑性エラストマーはスチレン−水素添加ポリオレフィン−スチレンブロック共重合体である請求項1〜4のいずれか1項に記載の塗装用マスキング材 The masking material for coating according to any one of claims 1 to 4, wherein the styrenic thermoplastic elastomer is a styrene-hydrogenated polyolefin-styrene block copolymer .
JP2001164643A 2000-10-11 2001-05-31 Masking material for painting Expired - Fee Related JP4953519B2 (en)

Priority Applications (11)

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JP2001164643A JP4953519B2 (en) 2000-10-11 2001-05-31 Masking material for painting
EP01974696A EP1332801A4 (en) 2000-10-11 2001-10-04 Masking material
CA002424080A CA2424080C (en) 2000-10-11 2001-10-04 A masking member
PCT/JP2001/008771 WO2002030580A1 (en) 2000-10-11 2001-10-04 Masking material
AU2001294189A AU2001294189B2 (en) 2000-10-11 2001-10-04 Masking material
CNB018172318A CN1209200C (en) 2000-10-11 2001-10-04 Masking material
US10/399,078 US7247366B2 (en) 2000-10-11 2001-10-04 Masking material
KR1020037005108A KR100791915B1 (en) 2000-10-11 2001-10-04 Masking material
AU9418901A AU9418901A (en) 2000-10-11 2001-10-04 Masking material
TW90124636A TW557232B (en) 2000-10-11 2001-10-05 Masking material
BR0201228-6A BR0201228A (en) 2001-05-31 2002-04-11 Covering Element

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JP2001164643A JP4953519B2 (en) 2000-10-11 2001-05-31 Masking material for painting

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